Choi BO, Chung KW, Cho HJ, Park KD, Lee KS, Kim SM, Sunwoo IN
- KMID: 2343145
-
J Korean Neurol Assoc.
-
2005 Apr;23(2):227-231.
BACKGROUND: Mutations in the myelin protein zero (MPZ) gene, which is located on chromosome 1q21-q22, is present in Charcot-Marie-Tooth disease type 1B (CMT1B), CMT type 2, Dejerine-Sottas syndrome, and congenital...